SI
SI
discoversearch

We've detected that you're using an ad content blocking browser plug-in or feature. Ads provide a critical source of revenue to the continued operation of Silicon Investor.  We ask that you disable ad blocking while on Silicon Investor in the best interests of our community.  If you are not using an ad blocker but are still receiving this message, make sure your browser's tracking protection is set to the 'standard' level.
Biotech / Medical : Biotech success, 2002 -- Ignore unavailable to you. Want to Upgrade?


To: Miljenko Zuanic who wrote (25)2/19/2002 8:19:11 PM
From: Miljenko Zuanic  Read Replies (1) | Respond to of 117
 
Maybe this is still way early, but oportunities are here.

Proc. Natl. Acad. Sci. USA, Vol. 99, Issue 4, 2344-2349, February 19, 2002
PNAS Online

Neurobiology
Embryonic stem cells develop into functional dopaminergic neurons after transplantation in a Parkinson rat model
Lars M. Björklund*,,, Rosario Sánchez-Pernaute*,,§, Sangmi Chung*,¶, Therese Andersson*,¶,, Iris Yin Ching Chen§, Kevin St. P. McNaught*,, Anna-Liisa Brownell*,§, Bruce G. Jenkins§, Claes Wahlestedt, Kwang-Soo Kim*,¶, and Ole Isacson*,,,**
* Udall Parkinson's Disease Research Center of Excellence, Neuroregeneration Laboratories, and ¶ Molecular Neurobiology Laboratory, McLean Hospital/Harvard Medical School, 115 Mill Street, Belmont, MA 02478; Departments of § Radiology and ** Neurology, Massachusetts General Hospital and Program in Neuroscience, Harvard Medical School, Boston, MA 02114; and Karolinska Institute, SE-17177 Stockholm, Sweden

Edited by Gerald D. Fischbach, Columbia University College of Physicians and Surgeons, New York, NY, and approved November 29, 2001 (received for review August 20, 2001)

Although implantation of fetal dopamine (DA) neurons can reduce parkinsonism in patients, current methods are rudimentary, and a reliable donor cell source is lacking. We show that transplanting low doses of undifferentiated mouse embryonic stem (ES) cells into the rat striatum results in a proliferation of ES cells into fully differentiated DA neurons. ES cell-derived DA neurons caused gradual and sustained behavioral restoration of DA-mediated motor asymmetry. Behavioral recovery paralleled in vivo positron emission tomography and functional magnetic resonance imaging data demonstrating DA-mediated hemodynamic changes in the striatum and associated brain circuitry. These results demonstrate that transplanted ES cells can develop spontaneously into DA neurons. Such DA neurons can restore cerebral function and behavior in an animal model of Parkinson's disease.